NCT07600177PHASE4Recruiting
Mavacamten to Aficamten Transition in Patients With Obstructive Hypertrophic Cardiomyopathy
Oregon Health and Science University
Start Date
5/5/2026
Completion Date
3/15/2027
Summary
This is an investigator-initiated two-center study. The goal of this study is to investigate the feasibility, safety and efficacy outcomes of a seamless transition from mavacamten to aficamten in patients with obstructive hypertrophic cardiomyopathy (oHCM).
Eligibility Criteria
Age Range: 18 years to 90 years
Inclusion Criteria:
* Documented history of oHCM with documented resting and/or Valsalva LVOT obstruction ≥ 50 mmHg who are currently receiving mavacamten commercially.
* Echo-derived LVEF ≥55% on mavacamten at the time of enrollment.
* Patient willing to consent for the study and undergo the study procedures.
Exclusion Criteria:
* Severe aortic stenosis or sub-aortic obstruction
* Known infiltrative or storage disorder causing cardiac hypertrophy that mimics HCM (eg, Noonan syndrome, Fabry disease, amyloidosis).
* History of LVEF \<30%.
* Paroxysmal atrial fibrillation (AF) with documented episode within 3 months.
* Atrial fibrillation (paroxysmal or permanent) not on systemic anticoagulation.
* Documented history of current obstructive coronary artery disease (\> 70% stenosis in one or more epicardial coronary arteries) or documented history of myocardial infarction.
Interventions
DRUG
Aficamten
Conditions
Hypertrophic Cardiomyopathy (HCM)
Locations
St. Luke's Hospital - Mid America Heart Institute
Kansas City, Missouri 64111
United States
Oregon Health & Science University
Portland, Oregon 97239
United States